Canonical Allele Identifier: CA910339549
Gene: CNTN3 HGNC NCBI

Linked Data

dbSNP Id: rs1344553718
MyVariant Identifiers: chr3:g.74627750A>T (hg19) chr3:g.74578599A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.74578599A>T , CM000665.2:g.74578599A>T GRCh38
NC_000003.11:g.74627750A>T , CM000665.1:g.74627750A>T GRCh37
NC_000003.10:g.74710440A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000263665.7:c.-81+35792T>A MANE Select ENSP00000263665.6:n.-81+35792T>A
XM_005264757.2:c.-81+35792T>A XP_005264814.1:n.-81+35792T>A
XM_005264758.2:c.-81+35792T>A XP_005264815.1:n.-81+35792T>A
XM_005264757.3:c.-81+35792T>A XP_005264814.1:n.-81+35792T>A
XM_017006507.1:c.-81+35149T>A XP_016861996.1:n.-81+35149T>A
NM_001393376.1:c.-81+35149T>A NP_001380305.1:n.-81+35149T>A
NM_020872.3:c.-81+35792T>A MANE Select NP_065923.1:n.-81+35792T>A
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